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Icon Clinical Research Jobs in Indiana (NOW HIRING)

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Icon Clinical Research information

See Indiana salary details

$46.6K

$102.1K

$179.8K

How much do icon clinical research jobs pay per year?

As of Aug 30, 2026, the average yearly pay for icon clinical research in Indiana is $102,137.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,100.00 and $116,600.00 per year, depending on experience, location, and employer.

What is an Icon Clinical Research?

An ICON Clinical Research job typically involves working for ICON plc, a global provider of outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies. Roles at ICON can range from clinical research associates and project managers to data analysts and regulatory specialists. Employees help design, manage, and monitor clinical trials to ensure they meet regulatory and ethical standards. These positions often require experience in clinical research, strong attention to detail, and adherence to Good Clinical Practice (GCP) guidelines.

What does a typical day look like for someone working at Icon Clinical Research?

A typical day at ICON Clinical Research often involves collaborating with cross-functional teams to oversee the progress of clinical trials, monitoring study data for accuracy, and ensuring all activities adhere to regulatory standards. You'll attend project meetings, communicate regularly with sponsors and investigators, and manage documentation and reporting tasks using specialized software. Depending on your specific role, you may also be responsible for site management, participant enrollment, or clinical data review. The work environment is fast-paced and supportive, offering opportunities for professional growth and advancement within the clinical research field.

What are the key skills and qualifications needed to thrive in the Icon Clinical Research position, and why are they important?

To thrive at ICON Clinical Research, you typically need a background in life sciences or a related field, experience with clinical trial processes, and strong analytical skills. Familiarity with industry-standard clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication help you excel in a collaborative research environment. These skills are crucial to ensure regulatory compliance, data integrity, and successful execution of clinical trials.

What are the most commonly searched types of Icon Clinical Research jobs in Indiana?

The most popular types of Icon Clinical Research jobs in Indiana are:

What are popular job titles related to Icon Clinical Research jobs in Indiana?

For Icon Clinical Research jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Icon Clinical Research jobs in Indiana look for?

The top searched job categories for Icon Clinical Research jobs in Indiana are:

What cities in Indiana are hiring for Icon Clinical Research jobs?

Cities in Indiana with the most Icon Clinical Research job openings:

Icon Clinical Research jobs near you
Infographic showing various Icon Clinical Research job openings in Indiana as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $102,137 per year, or $49.1 per hour.

Clinical Research Associate

Indianapolis, IN

Icon plc
See more jobs at Icon plcexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

Job description

Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required (approximately 60%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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